Primary Device ID | 00846338001094 |
NIH Device Record Key | 1e4d9db3-a6d0-41d4-8b6c-822dd7a845e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlexTrode® Malleable Electrode |
Version Model Number | FT-N/S |
Company DUNS | 019872358 |
Company Name | ELLIQUENCE, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00846338001094 [Primary] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-02-07 |
Device Publish Date | 2016-09-22 |
00846338001124 | FT-W/S |
00846338001117 | FT-S/S |
00846338001094 | FT-N/S |
00846338001087 | FT-L7/S |
00846338001070 | FT-L5/S |
00846338001063 | FT-L3/S |
00846338001056 | FT-D/S |
00846338001049 | FT-B3/S |
00846338001032 | FT-B2/S |
00846338001025 | FT-B1/S |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FLEXTRODE 77877857 4187161 Live/Registered |
Cosman, Eric Richard 2009-11-20 |
FLEXTRODE 74360607 1797701 Dead/Cancelled |
AMREX-ZETRON, INC. 1993-02-22 |
FLEXTRODE 73606651 1424722 Dead/Cancelled |
AMREX-ZETRON, INC. 1986-06-27 |